Clinical QC Associate II — On-Site Montreal, Growth & Benefits

Altasciences; Laval; On-site; CAD 55,000 - 75,000; Full time

Benefits offered by this job

Health/dental/vision insurance

RRSP with employer match

Paid vacation & statutory vacations

Paid sick leave & bereavement leave

Employee assistance & telehealth

Job summary

Altasciences is seeking a Clinical Quality Control Associate to perform QC reviews of clinical trial data in alignment with GCP and SOPs. The role collaborates with the Quality Systems team to ensure compliant task execution and data integrity.

Responsibilities include error tracking, deviation documentation, and mentoring the Quality Systems team, while maintaining strong communication with supervisors. English/French fluency is required and on-site duties are performed in Quebec.

Qualifications

• High School Diploma completed.
• Fluency in French and English.
• Detail oriented, well organized, customer service focused.
• Proficient with Microsoft Office.
• Ability to lift up to 25 pounds.
• Self-directed with initiative.

Responsibilities

• Report and elevate errors or trends that may require retraining (per location).
• Compile data and maintain computerized files and/or update deviation tracking systems.
• Record, track and ensure the resolution of data queries.
• Proactively communicate issues and resolutions to supervisors and managers.
• Ensure confidentiality of clinical trial participants and sponsors.
• Maintain high level of quality and customer service within the department.
• Document and/or report clinical trial related deviations (SOP, protocol).
• Act as a mentor and coach the Quality Systems team members.
• Understand protocol driven timed study events and acceptable collection windows.
• Perform other tasks as assigned by management.

Skills

French & English communication

Detail oriented

Organized

Customer service oriented

Lift 25 pounds

Self-directed

Microsoft Office

Education

High School Diploma

Tools

Microsoft Office

Job description

Altasciences is seeking a Clinical Quality Control Associate to perform QC reviews of clinical trial data in alignment with GCP and SOPs. The role collaborates with the Quality Systems team to ensure compliant task execution and data integrity.

Responsibilities include error tracking, deviation documentation, and mentoring the Quality Systems team, while maintaining strong communication with supervisors. English/French fluency is required and on-site duties are performed in Quebec.